Department of Pharmacology, Vascular Biology and Therapeutic Program, Yale University, New Haven, CT 06520, USA.
Department of Cellular and Molecular Physiology, Yale University, New Haven, CT 06520, USA; Nanobiology Institute, Yale University, New Haven, CT 06520, USA; Department of Molecular Biophysics and Biochemistry, Yale School of Medicine, Yale University, New Haven, CT 06520, USA.
Dev Cell. 2019 Apr 22;49(2):206-219.e7. doi: 10.1016/j.devcel.2019.02.023. Epub 2019 Mar 28.
Cell polarization is important for various biological processes. However, its regulation, particularly initiation, is incompletely understood. Here, we investigated mechanisms by which neutrophils break their symmetry and initiate their cytoskeleton polarization from an apolar state in circulation for their extravasation during inflammation. We show here that a local increase in plasma membrane (PM) curvature resulting from cell contact to a surface triggers the initial breakage of the symmetry of an apolar neutrophil and is required for subsequent polarization events induced by chemical stimulation. This local increase in PM curvature recruits SRGAP2 via its F-BAR domain, which in turn activates PI4KA and results in PM PtdIns4P polarization. Polarized PM PtdIns4P is targeted by RPH3A, which directs PIP5K1C90 and subsequent phosphorylated myosin light chain polarization, and this polarization signaling axis regulates neutrophil firm attachment to endothelium. Thus, this study reveals a mechanism for the initiation of cell cytoskeleton polarization.
细胞极化对于各种生物过程都很重要。然而,其调控机制,尤其是起始机制,尚不完全清楚。在这里,我们研究了中性粒细胞如何打破对称性,并在炎症期间从循环中的无极性状态出发,通过细胞与表面的接触,引发其细胞骨架极化,从而实现细胞外渗。我们在这里表明,细胞膜(PM)曲率的局部增加是由于细胞与表面接触而导致的,这种增加会触发无极性中性粒细胞对称性的初始破坏,并且是随后由化学刺激诱导的极化事件所必需的。这种 PM 曲率的局部增加通过其 F-BAR 结构域招募 SRGAP2,后者转而激活 PI4KA,导致 PM PtdIns4P 极化。极化的 PM PtdIns4P 被 RPH3A 靶向,后者指导 PIP5K1C90 和随后的磷酸化肌球蛋白轻链极化,并且这个极化信号轴调节中性粒细胞与内皮的牢固附着。因此,这项研究揭示了细胞骨架极化起始的一种机制。